ENST00000452035.7:n.2299T>A
|
|
|
ENST00000483004.2:c.1596T>A
|
ENSP00000419887.2:p.Thr532=
|
|
ENST00000698628.1:c.1625-243T>A
|
ENSP00000513848.1:n.1625-243T>A
|
|
ENST00000698629.1:n.2084T>A
|
|
|
ENST00000698630.1:n.2528T>A
|
|
|
ENST00000698631.1:n.2529T>A
|
|
|
ENST00000698632.1:n.3418T>A
|
|
|
ENST00000698633.1:n.3308T>A
|
|
|
ENST00000425368.7:c.1812T>A
MANE Select
|
ENSP00000416561.2:p.Thr604=
|
|
ENST00000425368.6:c.1812T>A
|
ENSP00000416561.2:p.Thr604=
|
|
ENST00000456570.5:c.3318T>A
|
ENSP00000410815.1:p.Thr1106=
|
|
ENST00000467360.1:n.938T>A
|
|
|
ENST00000477310.1:c.2865T>A
|
ENSP00000418996.1:p.Thr955=
|
|
ENST00000482312.1:n.28T>A
|
|
|
ENST00000483004.1:c.434T>A
|
|
|
NM_001710.5:c.1812T>A , LRG_136t1:c.1812T>A
|
NP_001701.2:p.Thr604=
|
|
NM_001710.6:c.1812T>A
MANE Select
|
NP_001701.2:p.Thr604=
|
|